Hs02722299_cn

• Gene Symbol: AVEN
• Assay Reference Genome Location: Chr.15:33866147 on build GRCh38
• Cytoband: 15q14

Target Gene Details

• Entrez Gene ID: 57099
• Gene Name: apoptosis and caspase activation inhibitor
• Gene Aliases: PDCD12
• Location: Chr.15:33858602-34074877 on Build GRCh38
• Assay Gene Location:

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
AVEN

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv471235	Chr.15:33743328 - 34129750 on Build GRCh38	Gain	CHRM5 PGBD4 AVEN RYR3 EMC7
nsv1052620	Chr.15:32612402 - 34538731 on Build GRCh38	Gain	NOP10 LPCAT4 SLC12A6 CHRM5 MIR1233-2 TMCO5B EMC7 KATNBL1 EMC4 NUTM1 LOC105370757 FMN1 PGBD4 GOLGA8B MIR1233-1 AVEN LOC101928042 RYR3 SCG5 ARHGAP11A GREM1 GOLGA8A LOC100131315 LOC101928134
esv33337	Chr.15:31689863 - 34575097 on Build GRCh38	Gain+Loss	NOP10 LPCAT4 LOC100653133 LOC105370940 WHAMMP1 MIR1233-2 TMCO5B EMC7 KATNBL1 EMC4 GOLGA8B ULK4P1 GOLGA8O GOLGA8N MIR1233-1 CHRNA7 GOLGA8K LOC101928042 SCG5 ARHGAP11A LOC100131315 LOC101928134 SLC12A6 CHRM5 NUTM1 LOC105370757 FMN1 PGBD4 AVEN RYR3 GREM1 LOC100996255 LOC101060588 GOLGA8A
esv3569431	Chr.15:33564570 - 35080307 on Build GRCh38	Gain	NOP10 LPCAT4 SLC12A6 CHRM5 MIR1233-2 AQR EMC7 KATNBL1 EMC4 NUTM1 GJD2 LOC101928174 ZNF770 PGBD4 GOLGA8B MIR1233-1 AVEN RYR3 ACTC1 GOLGA8A
nsv568921	Chr.15:33754434 - 33955421 on Build GRCh38	Gain	AVEN RYR3
nsv456789	Chr.15:33742220 - 34134417 on Build GRCh38	Gain	CHRM5 PGBD4 AVEN RYR3 EMC7
nsv1044844	Chr.15:33773323 - 34004628 on Build GRCh38	Loss	CHRM5 AVEN RYR3
dgv4456n54	Chr.15:32604149 - 34557061 on Build GRCh38	Gain	NOP10 LPCAT4 MIR1233-2 TMCO5B EMC7 KATNBL1 EMC4 GOLGA8B GOLGA8N MIR1233-1 LOC101928042 SCG5 ARHGAP11A LOC100131315 LOC101928134 SLC12A6 CHRM5 NUTM1 LOC105370757 FMN1 PGBD4 AVEN RYR3 GREM1 GOLGA8A

More Information

Additional Information:

For this assay, SNP(s) [rs116671589] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Non-exonic, DGV Variation